← Back to Clinical Trials
Recruiting NCT06183645

NCT06183645 Exploratory Study on Predicting CIDP Patients' Decline During IV Immunoglobulin Treatment Adaptation Feasibility.

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06183645
Status Recruiting
Phase
Sponsor Centre Hospitalier Universitaire de Liege
Condition Chronic Inflammatory Demyelinating Polyneuropathy
Study Type OBSERVATIONAL
Enrollment 40 participants
Start Date 2023-08-28
Primary Completion 2028-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 99 Years
Study Type OBSERVATIONAL
Interventions
Actimyo

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 40 participants in total. It began in 2023-08-28 with a primary completion date of 2028-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

ActiCIDP is a monocentric academic study. Patients with Chronic inflammatory demyelinating polyradiculoneuritis may be included on a voluntary basis. The investigators plan to include a group of approximately 40 patients with CIDP. The investigators have planned to assess patient every three months for a year. After each visit, participants will wear Actimyo for one month daily.

Eligibility Criteria

Inclusion Criteria: * Diagnosed with CIDP or possible CIDP based on 2021 EAN/PNS criteria2. * Treated with IVIg (≤1g/kg/3-8week) * Clinically Stable disease for 3 months (according to treating physician opinion). * No treatment withdrawal failure within 1 year * Age over 18 years Exclusion Criteria: * Significant cognitive or communication disorders * Surgery or serious traumatic injury ≤ 6 months * Non ambulant patient * Current participation to a therapeutic trial * Anti-myeline antibodies (anti-MAG) positive or nodo-paranodopathy * Other autoimmune disease that requires Corticosteroids, IVIg, Plasma Exchange treatment * Pregnancy or breastfeeding * Any other condition that, according to the investigator, could significantly interfere with patient evaluation or safety.

Contact & Investigator

Central Contact

Laurie Medard

✉ laurie.medard@citadelle.be

📞 043215584

Principal Investigator

Margaux Poleur, Dr

PRINCIPAL INVESTIGATOR

CHR Citadelle

Frequently Asked Questions

Who can join the NCT06183645 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 99 Years, studying Chronic Inflammatory Demyelinating Polyneuropathy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06183645 currently recruiting?

Yes, NCT06183645 is actively recruiting participants. Contact the research team at laurie.medard@citadelle.be for enrollment information.

Where is the NCT06183645 trial being conducted?

This trial is being conducted at Liège, Belgium.

Who is sponsoring the NCT06183645 clinical trial?

NCT06183645 is sponsored by Centre Hospitalier Universitaire de Liege. The principal investigator is Margaux Poleur, Dr at CHR Citadelle. The trial plans to enroll 40 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology